基础医学与临床 ›› 2017, Vol. 37 ›› Issue (8): 1108-1112.

• 研究论文 • 上一篇    下一篇

过表达miR-10b促进肺癌细胞系A549增殖

唐静,石中全,胡玲,李国利,冯晓灵,刘奉   

  1. 重庆三峡医药高等专科学校
  • 收稿日期:2016-07-19 修回日期:2016-09-29 出版日期:2017-08-05 发布日期:2017-07-17
  • 通讯作者: 刘奉 E-mail:2179695579@qq.com
  • 基金资助:
    重庆三峡医药高等专科学校校级苗圃工程;重庆市教委

miR-10b overexpression promotes the proliferation of lung cancer cell line A549

  • Received:2016-07-19 Revised:2016-09-29 Online:2017-08-05 Published:2017-07-17

摘要: 目的 探讨非小细胞肺癌(NSCLC)患者肺癌及癌旁组织中microRNA-10b(miR-10b)表达水平及miR-10b是否通过调控锌指转录蛋白基因(KLF4)对肺癌细胞系A549恶性化的影响。方法 40例NSCLC患者病理切片,原位杂交检测肺癌及癌旁组织中miR-10b的表达量;对肺癌细胞系A549转染miR-10b mimics后,CCK-8法检测肺癌细胞增殖;real-time PCR及Western blot检测KLF4 mRNA及蛋白水平;软琼脂克隆形成实验检测过表达miR-10b对A549细胞的肿瘤恶性化程度的影响。结果 肺癌细胞A549及肺癌组织中miR-10b的表达量分别高于正常肺上皮细胞16HBE及癌旁组织;过表达miR-10b模拟物的A549细胞中,KLF4蛋白水平显著下降(P<0.05);过表达的miR-10b可显著增加A549细胞的增殖速度及在软琼脂内的成瘤性。结论 miR-10b在不同类型细胞及组织中具有分布差异性、可能是通过抑制KLF4的表达促进肺癌细胞增殖及恶性化。

关键词: miR-10b, KLF4, 非小细胞肺癌, 增殖, 恶性化

Abstract: Objective To explore the expression of microRNA-10b (miR-10b) in patients with non-small cell lung cancer (NSCLC) and adjacent tissues, and to investigate the effect of miR-10b on the malignant change of lung cancer cell A549 by regulating the expression of Kruppel-like factor 4 (KLF4). Methods 40 patients with NSCLC were selected and used in situ hybridization, with detection of lung cancer and adjacent tissues of miR-10b expression; lung cancer cell A549 transfected miR-10b mimics, changes of CCK-8 assay was used to detect the proliferation of lung cancer cells; real time PCR and Western blot were used to examine the cell KLF4 mRNA and protein levels; soft agar colony formation assay was used to detect the expression of miR-10b on the proliferation of lung cancer cell A549 tumor malignant. Results Lung cancer A549 cells and lung cancer tissue of miR-10b expression were higher than that of normal lung epithelial 16HBE cells and cancer adjacent tissues; overexpression of miR-10b analogue in A549 cells, KLF4 protein levels decreased significantly, KLF4 mRNA level was not changed significantly; miR-10b expression significantly increased the growth of A549 cells. Conclusion The distribution of miR-10b in different cell types and tissues may be different, which may promote the proliferation and malignancy of lung cancer cells by inhibiting the expression of KLF4.

Key words: miR-10b, Kruppel-like factor 4, non-small cell lung cancer, proliferation, malignant

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